NDC 69097-844

Alfuzosin Hydrochloride extended release

Alfuzosin Hydrochloride

Alfuzosin Hydrochloride extended release is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Cipla Usa Inc.. The primary component is Alfuzosin Hydrochloride.

Product ID69097-844_497e0a60-9b09-4dcc-8cc6-1f13196f2db4
NDC69097-844
Product TypeHuman Prescription Drug
Proprietary NameAlfuzosin Hydrochloride extended release
Generic NameAlfuzosin Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-06-30
Marketing CategoryANDA / ANDA
Application NumberANDA090284
Labeler NameCipla USA Inc.
Substance NameALFUZOSIN HYDROCHLORIDE
Active Ingredient Strength10 mg/1
Pharm ClassesAdrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 69097-844-02

30 TABLET in 1 BOTTLE (69097-844-02)
Marketing Start Date2016-06-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69097-844-07 [69097084407]

Alfuzosin Hydrochloride extended release TABLET
Marketing CategoryANDA
Application NumberANDA090284
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-06-30

NDC 69097-844-05 [69097084405]

Alfuzosin Hydrochloride extended release TABLET
Marketing CategoryANDA
Application NumberANDA090284
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-30

NDC 69097-844-02 [69097084402]

Alfuzosin Hydrochloride extended release TABLET
Marketing CategoryANDA
Application NumberANDA090284
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-06-30

NDC 69097-844-12 [69097084412]

Alfuzosin Hydrochloride extended release TABLET
Marketing CategoryANDA
Application NumberANDA090284
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-06-30

Drug Details

Active Ingredients

IngredientStrength
ALFUZOSIN HYDROCHLORIDE10 mg/1

OpenFDA Data

SPL SET ID:3cc028d5-309f-4ce3-a2d7-5804ab57677d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 861132
    • UPC Code
  • 0369097844073

    • Pharmacological Class

    • Adrenergic alpha-Antagonists [MoA]
    • alpha-Adrenergic Blocker [EPC]
    • Adrenergic alpha-Antagonists [MoA]
    • alpha-Adrenergic Blocker [EPC]

    Medicade Reported Pricing

    69097084412 ALFUZOSIN HCL ER 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    69097084407 ALFUZOSIN HCL ER 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Alfuzosin Hydrochloride extended release" or generic name "Alfuzosin Hydrochloride"

    NDCBrand NameGeneric Name
    0440-5000Alfuzosin hydrochlorideAlfuzosin hydrochloride
    13668-021ALFUZOSIN HYDROCHLORIDEALFUZOSIN HYDROCHLORIDE
    29300-155Alfuzosin hydrochlorideAlfuzosin hydrochloride
    31722-302Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    33261-994Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    42291-110Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    43353-945Alfuzosin hydrochlorideAlfuzosin hydrochloride
    47335-956Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    55648-738Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    57237-114Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    60505-2850Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    61919-349ALFUZOSIN HYDROCHLORIDEALFUZOSIN HYDROCHLORIDE
    63629-2353Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    63629-2354Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    63629-7907Alfuzosin hydrochlorideAlfuzosin hydrochloride
    63629-9155Alfuzosin hydrochlorideAlfuzosin hydrochloride
    63629-9295Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    64679-738Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    65862-249Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    69097-844Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    70934-306Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    70934-961Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    71335-1529Alfuzosin HydrochlorideAlfuzosin Hydrochloride
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.